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MicroRNA-532-5p protects against atherosclerosis through inhibiting vascular smooth muscle cell proliferation and migration.

Authors :
Sun H
Wu S
Sun B
Source :
Cardiovascular diagnosis and therapy [Cardiovasc Diagn Ther] 2020 Jun; Vol. 10 (3), pp. 481-489.
Publication Year :
2020

Abstract

Background: The present study aimed to explore the expression and clinical value of miR-532-5p in atherosclerosis (AS) patients, and analyze its regulating effect on biological behaviors of vascular smooth muscle cells (VSMCs).<br />Methods: A total of 103 AS patients and 77 healthy controls were included. The expression level of miR-532-5p was measured using quantitative real-time PCR (qRT-PCR). A receiver operating characteristic (ROC) analysis was counted to assess the diagnostic value of miR-532-5p in AS. CCK-8 and Transwell assay were used to detect the role of miR-532-5p in VSMCs proliferation and migration.<br />Results: MiR-532-5p was downregulated in AS patients compared with that in healthy controls. Serum miR-532-5p was inversely related to the carotid intima-media thickness (CIMT) in AS patients. A ROC curve was conducted with an area under the curve (AUC) of 0.897, with high sensitivity and specificity. Overexpression of miR-532-5p inhibited cell proliferation and migration in VSMCs, whereas miR-532-5p downregulation had a reverse effect.<br />Conclusions: Decreased expression of miR-532-5p might be a potential diagnostic biomarker for AS. Overexpression of miR-532-5p inhibits the proliferation and migration of VSMCs. The present results indicate a therapeutic potential of miR-532-5p for AS.<br />Competing Interests: Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/cdt-20-91). The authors have no conflicts of interest to declare.<br /> (2020 Cardiovascular Diagnosis and Therapy. All rights reserved.)

Details

Language :
English
ISSN :
2223-3652
Volume :
10
Issue :
3
Database :
MEDLINE
Journal :
Cardiovascular diagnosis and therapy
Publication Type :
Academic Journal
Accession number :
32695627
Full Text :
https://doi.org/10.21037/cdt-20-91